Acceptability and tolerability of repeated intramuscular electroporation of Multi-antigenic HIV (HIVMAG) DNA vaccine among healthy African participants in a phase 1 randomized controlled trial.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 19 08 2019
accepted: 24 04 2020
entrez: 30 5 2020
pubmed: 30 5 2020
medline: 4 8 2020
Statut: epublish

Résumé

Intramuscular electroporation (IM/EP) is a vaccine delivery technique that improves the immunogenicity of DNA vaccines. We evaluated the acceptability and tolerability of electroporation among healthy African study participants. Forty-five participants were administered a DNA vaccine (HIV-MAG) or placebo by electroporation at three visits occurring at four week-intervals. At the end of each visit, participants were asked to rate pain at four times: (1) when the device was placed on the skin and vaccine injected, before the electrical stimulation, (2) at the time of electrical stimulation and muscle contraction, and (3) at 10 minutes and (4) 30 minutes after the procedure was completed. For analyses, pain level was dichotomized as either "acceptable" (none/slight/uncomfortable) or "too much" (Intense, severe, and very severe) and examined over time using repeated measures models. Optional brief comments made by participants were summarized anecdotally. All 45 participants completed all three vaccination visits; none withdrew from the study due to the electroporation procedure. Most (76%) reported pain levels as acceptable at every time point across all vaccination visits. The majority of "unacceptable" pain was reported at the time of electrical stimulation. The majority of the participants (97%) commented that they preferred electroporation to standard injection. Repeated intramuscular electroporation for vaccine delivery was found to be acceptable and feasible among healthy African HIV vaccine trial participants. The majority of participants reported an acceptable pain level at all vaccination time points. Further investigation may be warranted into the value of EP to improve immunization outcomes. ClinicalTrials.gov NCT01496989.

Identifiants

pubmed: 32469893
doi: 10.1371/journal.pone.0233151
pii: PONE-D-19-22032
pmc: PMC7259687
doi:

Substances chimiques

AIDS Vaccines 0
Vaccines, DNA 0

Banques de données

ClinicalTrials.gov
['NCT01496989']

Types de publication

Clinical Trial, Phase I Journal Article Multicenter Study Randomized Controlled Trial Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0233151

Subventions

Organisme : NIMH NIH HHS
ID : R25 MH064712
Pays : United States
Organisme : NIMH NIH HHS
ID : R25 MH123256
Pays : United States

Déclaration de conflit d'intérêts

PEF, MP and FP were employees of IAVI at the time of the study. DH is an employee of Ichor Medical Sciences Inc which owns the rights to the TriGrid Delivery System. The rest of the authors have no competing interests.

Références

PLoS One. 2015 Aug 07;10(8):e0134287
pubmed: 26252526
Nat Rev Genet. 2008 Oct;9(10):776-88
pubmed: 18781156
Mol Ther Methods Clin Dev. 2016 Aug 31;3:16061
pubmed: 27617268
J Infect Dis. 2013 Sep 1;208(5):818-29
pubmed: 23840043
Vaccine. 2011 Jan 17;29(4):795-803
pubmed: 21094270
Hum Vaccin Immunother. 2013 Oct;9(10):2246-52
pubmed: 24051434
Vaccine. 2007 May 16;25(20):4085-92
pubmed: 17391815
Sex Transm Infect. 2007 Oct;83(6):426-32
pubmed: 17911142
Mol Ther. 2009 May;17(5):922-8
pubmed: 19277016
Pediatr Infect Dis J. 2013 Jul;32(7):777-85
pubmed: 23838777
J Infect Dis. 2006 Dec 15;194(12):1650-60
pubmed: 17109336
PLoS One. 2015 Jun 29;10(6):e0131748
pubmed: 26121679
PLoS One. 2011;6(5):e19252
pubmed: 21603651
Mol Ther. 2012 Jan;20(1):214-20
pubmed: 22068424

Auteurs

Juliet Mpendo (J)

Uganda Virus Research Institute-International AIDS Vaccine Initiative, HIV Vaccine Program, Entebbe, Uganda.

Gaudensia Mutua (G)

Kenya AIDS Vaccine Initiative, University of Nairobi, Nairobi, Kenya.

Annet Nanvubya (A)

Uganda Virus Research Institute-International AIDS Vaccine Initiative, HIV Vaccine Program, Entebbe, Uganda.

Omu Anzala (O)

Kenya AIDS Vaccine Initiative, University of Nairobi, Nairobi, Kenya.

Julien Nyombayire (J)

Project San Francisco (PSF), Kigali, Rwanda.

Etienne Karita (E)

Project San Francisco (PSF), Kigali, Rwanda.

Len Dally (L)

EMMES Corporation, Rockville, Maryland, United States of America.

Drew Hannaman (D)

Ichor Medical Systems, Inc., San Diego, California, United States of America.

Matt Price (M)

International AIDS Vaccine Initiative (IAVI), New York, NY, United States of America.

Patricia E Fast (PE)

International AIDS Vaccine Initiative (IAVI), New York, NY, United States of America.

Frances Priddy (F)

International AIDS Vaccine Initiative (IAVI), New York, NY, United States of America.

Huub C Gelderblom (HC)

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, United States of America.

Nancy K Hills (NK)

University of California at San Francisco, San Francisco, California, United States of America.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH